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Phospho-p70 S6 Kinase Alpha (Ser447) Polyclonal Antibody

SKU: E-AB-20959-200

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Phospho-p70 S6 Kinase Alpha (Ser447) Polyclonal Antibody

 

SKU # E-AB-20959
Reactivity Human,  Mouse,  Rat
Host Rabbit
Applications WB,  IHC-p

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC-p
Clonality Polyclonal
Immunogen Synthesized peptide derived from human p70 S6 kinase α around the phosphorylation site of Ser447
Synonyms 70 kDa ribosomal protein S6 kinase 1,  KS6B1,  P70 S6 Kinase,  P70 beta 1,  alpha 1,  alpha 2,  p70 S6 kinase,  p70 S6 kinase alpha,  p70 S6K,  p70 S6K-alpha,  p70 S6KA,  p70 alpha,  p70 ribosomal S6 kinase alpha,  p70 ribosomal S6 kinase beta 1,  p70(S6,  p70(S6K) alpha
Swissprot
Calculated MW 59 kDa
Observed MW 60 kDa
Cellular Localization Cytoplasm, Nucleus, Cytoplasm and Cell junction>synapse>synaptosome, Mitochondrion outer membrane.
Tissue Specificity Widely expressed
Concentration 1 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 0.5% protein protectant and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Cell Biology,  Epigenetics and Nuclear Signaling,  Metabolism,  Signal Transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
WB 1:500-1:2000
IHC 1:100-1:300

 

Background   

P70 S6 Kinase alpha is a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases and contains 2 non-identical kinase catalytic domains. It phosphorylates several residues of the S6 ribosomal protein. The kinase activity of this protein is activated by serine/threonine phosphorylation and protein kinase C and inactivated by type 2A phosphatase. Activation leads to an increase in protein synthesis and cell proliferation. Overexpression of this kinase is involved in some breast cancer cell lines. Alternate translational start sites have been described and alternate transcriptional splice variants have been observed but have not been thoroughly characterized.